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BAF312
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
BAF312图片
CAS NO:1230487-00-9
包装:5mg, 10mg, 50mg
包装与价格:
包装价格(元)
5mg电议
10mg电议
50mg电议

产品名称
Siponimod
产品介绍

生物活性

BAF312 (Siponimod) is a next-generation S1P receptor modulator, selective for S1P1 and S1P5 receptors with EC50 of 0.39 nM and 0.98 nM, exhibits >1000-fold selectivity over S1P2, S1P3 and S1P4 receptors.


化学数据

分子量516.6
分子式C29H35F3N2O3
CAS号1230487-00-9
纯度>99%
溶解性(25°C)DMSO ≥ 30 mg/mL
储存和运输条件固体粉末: -20°C 冷藏长期储存
常温运输及临时存放

实验操作 来自于公开的文献,仅供相同实验参考(如实验材料、目的不同,请参考其他文献)

细胞实验
细胞系CHO cells
方法Agonist-mediated internalization of S1P1 receptors in CHO cells analysed by flow cytometry
Myc-tag hS1P1 cells were incubated for 1 h with agonist at 37°C in standard culture medium followed by a PBS wash. An aliquot was kept on ice for 3 h, while another aliquot was left for 3 (or 12) h in culture medium (no agonist) at 37°C. The cells were then incubated either with 4 μg·mL–1 monoclonal mouse anti C-myc IgG1 (Roche Applied Science, Mannheim, Germany) antibody or with isotype control mouse IgG1 (Pharmingen, BD Biosciences, Basel, Switzerland) for 60 min at 4°C, followed by an incubation with 1 μg·mL–1 of Alexa488-labelled goat anti-mouse secondary conjugates (Molecular Probes, Juro Supply, Luzern, Switzerland). The cells were subjected to flow cytometry measurements using 10000 viable cells per sample.
浓度1 μM
处理时间1h

动物实验
动物模型EAE model in the DA rat
配制1% aqueous carboxy-methylcellulose (C-4888, Sigma Chemical Co, St Louis, MO)
剂量0.03, 0.3 and 3 mg/kg once daily
给药处理oral gavage

不同实验动物依据体表面积的等效剂量转换表(数据来源于FDA指南)

小鼠大鼠豚鼠仓鼠
重量 (kg)0.020.151.80.40.0810
体表面积 (m2)0.0070.0250.150.050.020.5
Km系数36128520
动物 A (mg/kg) = 动物 B (mg/kg) × 动物 B的Km系数
动物 A的Km系数

例如,依据体表面积折算法,将化合物用于小鼠的剂量20 mg/kg 换算成大鼠的剂量,需要将20 mg/kg 乘以小鼠的Km系数(3),再除以大鼠的Km系数(6),得到化合物用于大鼠的等效剂量为10 mg/kg。


储备液配制

以下数据基于产品分子量,对于特殊产品,请参照COA中的储备液配制条件和说明进行操作。

Concentration / Solvent Volume / Mass1 mg5 mg10 mg
1 mM1.9357 mL9.6787 mL19.3573 mL
5 mM0.3871 mL1.9357 mL3.8715 mL
10 mM0.1936 mL0.9679 mL1.9357 mL